Hybridisation In Chemistry | Hybridisation Examples

Hybridization in Chemistry

In chemistry, hybridisation may be defined as the mixing of two or more than two atomic orbitals of an atom, having comparable energy, to give an equal number of identical orbitals having same energy and shape. All hybrid orbitals are oriented symmetrically to have a maximum distance from each other.

The Chemistry of Hybridisation in Methane, Ethylene and Acetylene

Thus, the molecule of methane can be represented by the overlap of a hydrogen 1s orbital with each of the four sp3 orbitals of carbon. The chemistry of hybrid orbitals formed by hybridisation of orbitals of other molecules may similarly be represented.

Linear combination of a 2s and two of the 2p orbitals, for example in ethylene, gives rise to three trigonal sp2 orbitals directed towards the corners of an equilateral triangle. The plane defined by the two original 2p orbitals leaves the remaining 2p orbitals, perpendicular to the plane of the triangle.

The planar structure of methyl radical can be represented by the overlap of each of the three sp2 orbitals of carbon with an s orbital of hydrogen, forming three C-H bonds, leaving the odd electron on the third unhybridized 2p orbital free.

 Likewise, hybridization of an s and p orbital gives two diagonal (sp) orbitals, directed towards the opposite ends of the line defined by the p orbital.

Methane, ethylene and acetylene are the classic examples of sp3, sp2 and sp hybridized carbon atom, respectively. The pictorial representation of hybridized orbitals of methane is given.

Hybridisation In Ethylene

Ethylene is represented by two carbon atoms combining through two sp2 orbitals, and overlapping of the remaining two sp2  orbitals on each carbon atom with 1s orbitals of two hydrogen atoms. The unhybridized parallel 2p orbitals, one on each of the trigonal carbon atoms overlap each other sideways to form a π bond. The electrons involved in such a bonding are called π-electrons. The π-electron cloud (pi bond) is distributed above and below the plane of the molecule, which is the nodal plane of the pi cloud.

The bond energy of the carbon-carbon pi bond is about 60 kcal or 250.8 kJ, and, is, therefore, weaker than a C-C sigma bond which is 83 kcal or 346.9 kJ of energy. As the carbon atoms are held more tightly, the carbon-carbon bond distance in ethylene is shorter (1.34 Angstrom) than the C-C sigma bond length in ethane (1.54 Angstrom). The angle between the bonds is 120o, and the molecule is planar.

Hybridisation In Acetylene

Likewise, in acetylene, as represented in the fig., each carbon atom is bonded diagonally to two other atoms, a carbon and hydrogen, through the overlap of two sp-hybridised orbitals of the carbon atoms, and of the remaining two sp orbitals of carbon atoms with two 1s orbitals of hydrogen. This leaves two p orbitals on each carbon atom, perpendicular to each other, as also to the sp hybrid orbital. The sideways overlap of the two parallel pairs of p orbitals leads to the formation of two π bonds, which merge into something like a cylindrical π electron cloud.

 

 

 

Hybridization and Bond Properties In Chemistry:

Bond properties, such as bond length and bond energy, are greatly influenced by the state of hybridization in which the atom exists.

An s orbital is at a lower level than a p atomic orbital (AO), which is at a lower level than a d AO. Therefore, the greater the s contribution in the hybrid AOs of the valence state, the greater is the electronegativity of the atom relative to a second atom is determined by the electronegativity of the hybridized AO with which they enter into bonding.

The dissociation energy of a bond increases with the difference in electronegativities of the bonded atoms. Therefore, it depends on the state of hybridization of the bonded atoms.

The electronegativity of carbon is greatest in sp hybridized state and least in sp3 state. As a result, the C-H bond formed with a carbon orbital of high p-character. The change in hybridization of AOs in carbon, thus, produces a change in the size of covalent atomic radius, decreasing from the tetrahedral (sp3) to the diagonal type (sp).

In fact, the state of hybridization in which the bonded atoms exist is the most important factor in determining bond length.

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